Laser desorption/vacuum ultraviolet photoionization of alkanethiolate self-assembled monolayers

被引:0
|
作者
Trevor, JL
Hanley, L
Lykke, KR
机构
[1] UNIV ILLINOIS,DEPT CHEM,CHICAGO,IL 60607
[2] ARGONNE NATL LAB,DIV CHEM & MAT SCI,ARGONNE,IL 60439
[3] NATL INST STAND & TECHNOL,OPT TECHNOL DIV,GAITHERSBURG,MD 20899
关键词
D O I
10.1002/(SICI)1097-0231(199704)11:6<587::AID-RCM877>3.0.CO;2-J
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Self assembled monolayers of straight-chain alkanethiolates (RS) on gold were studied by nitrogen laser desorption followed by vacuum ultraviolet (118 nm) photoionization of secondary neutrals in a time-of-flight mass spectrometer. The dominant feature of all photoionization mass spectra were the dimers (RSSR+) for all thiolates studied. No monomer ions (RS') were observed, in contrast with previous results from time-of-flight secondary ion and direct laser desorption mass spectrometry. Results are presented from experiments on the tetradecyl (C-14) and hexadecyl (C-16) mercaptan monolayers. Mixed C-14/C-16 monolayers generated both pure and mixed dimers, indicating a facile association between different monomer chain lengths. (C) 1997 by John Whey & Sons, Ltd.
引用
收藏
页码:587 / 589
页数:3
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